[Federal Register Volume 86, Number 99 (Tuesday, May 25, 2021)]
[Notices]
[Page 28153]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-10995]


-----------------------------------------------------------------------

DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-838]


Importer of Controlled Substances Application: SpecGX, LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

-----------------------------------------------------------------------

SUMMARY: SpecGX, LLC. has applied to be registered as an importer of 
basic class(es) of controlled substance(s). Refer to Supplemental 
Information listed below for further drug information.

DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may file written comments on or objections to 
the issuance of the proposed registration on or before June 24, 2021. 
Such persons may also file a written request for a hearing on the 
application on or before June 24, 2021.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DPW, 
8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a 
hearing must be sent to: Drug Enforcement Administration, Attn: 
Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All 
requests for a hearing should also be sent to: (1) Drug Enforcement 
Administration, Attn: Hearing Clerk/OALJ, 8701 Morrissette Drive, 
Springfield, Virginia 22152; and (2) Drug Enforcement Administration, 
Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, 
Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this 
is notice that on February 5, 2021, SpecGX LLC, 3600 North 2nd Street, 
Saint Louis, Missouri 63147, applied to be registered as an importer of 
the following basic class(es) of controlled substance(s):

------------------------------------------------------------------------
                                           Drug
          Controlled substance             code          Schedule
------------------------------------------------------------------------
Marihuana...............................    7360  I
Phenylacetone...........................    8501  II
Coca Leaves.............................    9040  II
Thebaine................................    9333  II
Opium, Raw..............................    9600  II
Poppy Straw Concentrate.................    9670  II
Tapentadol..............................    9780  II
------------------------------------------------------------------------

    The company plans to import the listed controlled substances for 
bulk manufacture into Active Pharmaceutical Ingredients (API) for 
distribution to its customers. In reference to Tapentadol (9780) and 
Thebaine (9333), the company plans to import intermediate forms of 
these controlled substances for further manufacturing prior to 
distribution to its customers. In reference to drug code 7360 
(Marihuana), the company plans to import synthetic cannabinol. No other 
activity for this drug is authorized for this registration. Placement 
of these codes onto the company's registration does not translate into 
automatic approval of subsequent permit applications to import 
controlled substances.
    Approval of permit applications will occur only when the 
registrant's business activity is consistent with what is authorized 
under 21 U.S.C. 952(a)(2).
    Authorization will not extend the import of Food and Drug 
Administration-approved or non-approved finished forms for commercial 
sale.

William T. McDermott,
Assistant Administrator.
[FR Doc. 2021-10995 Filed 5-24-21; 8:45 am]
BILLING CODE P